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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594284Generated: October 25, 2026

Dimethylformamide → Dibenzo(b,d)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/594284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-BromodibenzothiopheneHCID 299508—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductDibenzo(b,d)thiophene-2-carbaldehydeHCID 641360—

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) suspension of commercially available 2-bromodibenzo[b,d]thiophene (500 mg; 1.90 mmol) in anh. Et2O (5 ml), under nitrogen, was treated dropwise with a solution of 1.6 M n-BuLi in hexanes (1.26 ml; 2.01 mmol). The resulting suspension was further stirred at 0° C. for 30 min. Anh. DMF (0.156 ml; 2.03 mmol) was then added, and the mixture was stirred at rt for 20 min. Aq. sat. NH4Cl and Et2O were successively added, and the aq. layer was further extracted with Et2O. The mixed organic layers were washed with water, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM) afforded dibenzo[b,d]thiophene-2-carbaldehyde as an off-white solid. LC-MS (conditions A): tR=0.87 min.; no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-7ac324d6fe2c4573bcdca021ee6c52fc
Source noteuspto-grants-2016_01